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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709662Generated: November 1, 2026

N-bromobutanimide → 5-(Bromomethyl)-2-chlorobenzonitrile

https://huagongshe.com/reaction/1709662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Chloro-5-methylbenzonitrileHCID 12557200—
CatalystBenzoyl PeroxideHCID 7187—
SolventBenzeneHCID 241—
Product5-(Bromomethyl)-2-chlorobenzonitrileHCID 1403303530.4%

Reaction Steps

A mixture of 2-chloro-5-methylbenzonitrile (10.6 g, 69.9 mmol), N-bromosuccinimide (12.2 g, 68.5 mmol), and dibenzoyl peroxide (349 mg, 1.44 mmol) in benzene (350 ml) was refluxed 1.5 hours, cooled, and evaporated to dryness under vacuum. The residue was suspended in 7:3 (v/v) hexane-dichloromethane, filtered, and evaporated. The crude product was chromatographed on silica gel (650 g) eluted with 7:3 (v/v) hexane-dichloromethane to provide 4.8 g (30%) 4-chloro-3-cyanobenzyl bromide, m.p. 55°-58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950673
Source datasetuspto-grants-1990_08
ORD IDord-a87c250ef91449c1ba95a28514ddbcab
Source noteuspto-grants-1990_08